CA1165748A - Synthetic chemical absorbents - Google Patents
Synthetic chemical absorbentsInfo
- Publication number
- CA1165748A CA1165748A CA000378006A CA378006A CA1165748A CA 1165748 A CA1165748 A CA 1165748A CA 000378006 A CA000378006 A CA 000378006A CA 378006 A CA378006 A CA 378006A CA 1165748 A CA1165748 A CA 1165748A
- Authority
- CA
- Canada
- Prior art keywords
- phenol resin
- resin foamed
- celled
- plastic particles
- acids
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000000126 substance Substances 0.000 title description 20
- 239000002250 absorbent Substances 0.000 title 1
- 230000002745 absorbent Effects 0.000 title 1
- 239000004033 plastic Substances 0.000 claims abstract description 48
- 229920003023 plastic Polymers 0.000 claims abstract description 48
- 239000005011 phenolic resin Substances 0.000 claims abstract description 39
- 239000002245 particle Substances 0.000 claims abstract description 31
- 239000002253 acid Substances 0.000 claims abstract description 27
- 238000000034 method Methods 0.000 claims abstract description 26
- 239000007788 liquid Substances 0.000 claims abstract description 24
- 239000000463 material Substances 0.000 claims abstract description 18
- 150000007513 acids Chemical class 0.000 claims abstract description 17
- 238000012856 packing Methods 0.000 claims abstract description 14
- 150000001298 alcohols Chemical class 0.000 claims abstract description 13
- 230000002285 radioactive effect Effects 0.000 claims abstract description 12
- 239000004745 nonwoven fabric Substances 0.000 claims abstract description 6
- 239000004677 Nylon Substances 0.000 claims abstract description 4
- 229920001778 nylon Polymers 0.000 claims abstract description 4
- 239000012634 fragment Substances 0.000 claims abstract description 3
- 239000011230 binding agent Substances 0.000 claims description 8
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 4
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 2
- 238000005192 partition Methods 0.000 claims 2
- 150000007529 inorganic bases Chemical class 0.000 claims 1
- 150000007530 organic bases Chemical class 0.000 claims 1
- 239000000843 powder Substances 0.000 abstract description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 7
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 239000003463 adsorbent Substances 0.000 description 3
- 239000003518 caustics Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- 238000006386 neutralization reaction Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 231100001261 hazardous Toxicity 0.000 description 2
- 239000010451 perlite Substances 0.000 description 2
- 235000019362 perlite Nutrition 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 229940001593 sodium carbonate Drugs 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 235000017550 sodium carbonate Nutrition 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 239000010455 vermiculite Substances 0.000 description 2
- 235000019354 vermiculite Nutrition 0.000 description 2
- 229910052902 vermiculite Inorganic materials 0.000 description 2
- 101100345589 Mus musculus Mical1 gene Proteins 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- 239000011358 absorbing material Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000002730 additional effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000012459 cleaning agent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003223 protective agent Substances 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 230000002226 simultaneous effect Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 230000002311 subsequent effect Effects 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/36—After-treatment
- C08J9/40—Impregnation
- C08J9/42—Impregnation with macromolecular compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/02—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/02—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography
- B01D53/04—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography with stationary adsorbents
- B01D53/0407—Constructional details of adsorbing systems
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/22—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising organic material
- B01J20/26—Synthetic macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/32—Materials not provided for elsewhere for absorbing liquids to remove pollution, e.g. oil, gasoline, fat
-
- G—PHYSICS
- G21—NUCLEAR PHYSICS; NUCLEAR ENGINEERING
- G21F—PROTECTION AGAINST X-RADIATION, GAMMA RADIATION, CORPUSCULAR RADIATION OR PARTICLE BOMBARDMENT; TREATING RADIOACTIVELY CONTAMINATED MATERIAL; DECONTAMINATION ARRANGEMENTS THEREFOR
- G21F9/00—Treating radioactively contaminated material; Decontamination arrangements therefor
- G21F9/04—Treating liquids
- G21F9/06—Processing
- G21F9/12—Processing by absorption; by adsorption; by ion-exchange
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2251/00—Reactants
- B01D2251/60—Inorganic bases or salts
- B01D2251/606—Carbonates
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2253/00—Adsorbents used in seperation treatment of gases and vapours
- B01D2253/20—Organic adsorbents
- B01D2253/202—Polymeric adsorbents
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2253/00—Adsorbents used in seperation treatment of gases and vapours
- B01D2253/25—Coated, impregnated or composite adsorbents
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2257/00—Components to be removed
- B01D2257/70—Organic compounds not provided for in groups B01D2257/00 - B01D2257/602
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2257/00—Components to be removed
- B01D2257/93—Toxic compounds not provided for in groups B01D2257/00 - B01D2257/708
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2375/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
- C08J2375/04—Polyurethanes
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S210/00—Liquid purification or separation
- Y10S210/918—Miscellaneous specific techniques
- Y10S210/922—Oil spill cleanup, e.g. bacterial
- Y10S210/924—Oil spill cleanup, e.g. bacterial using physical agent, e.g. sponge, mop
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Analytical Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Materials Engineering (AREA)
- Public Health (AREA)
- Environmental & Geological Engineering (AREA)
- Physics & Mathematics (AREA)
- General Engineering & Computer Science (AREA)
- High Energy & Nuclear Physics (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Absorbent Articles And Supports Therefor (AREA)
- Laminated Bodies (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Abstract
ABSTRACT OF THE DISCLOSURE
A method of absorbing bases, acids, alcohols and radioactive liquids using phenol resin foamed plastic particles. The size of the particles should lie between about 0.25 and 70mm. They may be powdered open-celled or close-celled. They may be treated with an acid for absorbing a base, or with a base for absorbing an acid. A preferred use is in the form of packing material. The particles may be disposed in the form of of powder or flakes in liquid-permeable padding. The padding may be composed of a plastic web, in particular a nylon web, or of a non-woven fabric.
As packing material the phenol resin foamed plastic may be in the form of sheets, blocks, cubes, tablets, balls or fragments.
A method of absorbing bases, acids, alcohols and radioactive liquids using phenol resin foamed plastic particles. The size of the particles should lie between about 0.25 and 70mm. They may be powdered open-celled or close-celled. They may be treated with an acid for absorbing a base, or with a base for absorbing an acid. A preferred use is in the form of packing material. The particles may be disposed in the form of of powder or flakes in liquid-permeable padding. The padding may be composed of a plastic web, in particular a nylon web, or of a non-woven fabric.
As packing material the phenol resin foamed plastic may be in the form of sheets, blocks, cubes, tablets, balls or fragments.
Description
~ 1~5748 _BAOKGROUND OF THE INVENTION
The use of porous, hardened synthetic resin plastics obtained through the condensation of aminoplastic-or phenoplastically-formed compounds and aldehydes for the cleaning of organic solvents, which had been used as wash liquid for textile fabrics, is known from German patent DE-PS 1 132 545. For this purpose the foamed plastic acts as a filter, which absorbs the grease, odorous substances and finishing preparations washed by these solvents from the fabrics, but not the solvent cleaning agents themselves, in particular carbon tetrachloride, trichoroethylene, tetra-chloroethylene, benzol or benzene.
It has also already been suggested to use ground formalehyde resin or phenol resin foamed plastic for the absorbing and binding of oil, benzene, fat or other such chemical substances.
For purposes of catastrophe protection and other such necessary cases, to prevent acids or bases from doing harm, acids for example will be treated with sodium carbonate and thereby neutralized. This treatment with sodium carbon-ate makes it possible in many cases to add too much soda, whereby an excess of chemical caustic is then present. The neutralized product is bound by means of inorganic substances having h-igh absorption capacity. These inorganic substances with highabsorptioncapacity resulting from their containing a plurality of fine porous cells are e.g.
perlite, kieselguhr or vermiculite. The treating of a base with an acid or an acid with a base requires in addition to knowledge of chemical procedures a great deal of caution and accuracy, so that no dangerous reactions occur. Various products appear, depending on the chemicals to be neutralized, including dangerous or hazardous fumes.
~ 1 _ ~ 165748 Until now neutralization or setting of hazardous acids and bases by inorganic high porosity materials, such as the mentioned perlite, kieselguhr or vermiculite, have the further disadvantages that these materials cannot be destroyed or are destroyed only with great difficulty, since they are not combustible at customary combustion temperatures, in particular being not combustible without residue. Thus upon their subseq-uent storage or deposition the material, furthermore containing absorbed substances, as a result of the effect of water upon the substances which were initially absorbed, releases these substances whereby an additional danger is present.
The present invention is thus based upon the problem of selecting a chemical adsorbent which with an extremely high absorbing volume harmlessly takes up and unbinds acids and bases and at the same time may be destroyed through combustion practically free of residue.
SUMMARY OF THE INVENTION
In order to solve this problem, the use of phenol resin foamed plastic particles is proposed for the absorptionof bases, alcohols and radioactive liquids and acids. In addition to liquids, they can also treat such constituents which are other-wise absorbable or adherable in the foamed plastic particles.
Phenol resin foamed plastic has the capacity of absorbing and binding a large plurality of various bases and caustics to a high degree, without thereby becoming corroded to such a degree that the absorbing capacity or retaining capacity of the absorbing material suffers. The acids or bases can be of both inorganic and organic types. The phenol resin foamed plastic is also excellently suitable for the absorbing of alcohols, and even for holding radioactive liquids. A homogeneous subst-ance is accordingly capable of safely absorbing and retaining J
~ 165i48 various liquids.
In accordance with a particular embodiment of the present invention, it is suggested that a phenol resin foamed plast;c for absorbing a base be treated with an acid or be provided with accumulated acid particles, whereas a phenol resin foamed plastic destined for absorbing an acid should be treated with a base or display basic elements in its hol-low spaces, so that the neutralization of the mentioned sub-stances occurs with or within the foamed plastic. Thus a phenol resin powder or granulate for an acid neutralization in particular, is advantageously mixed with calcium carbonate.
In a a further embodiment according to the presen~
invention, it is suggested that the mentioned phenol resin foamed plastic particles be used as packing material.
According to an additional embodiment of the present invention the phenol resin foamed plastic particles in the form of powder or flakes are disposed in liquid-permeable padding, which is composed of a plastic web, in 20 particular a nylon web, or a non-woven fabric. In order to demonstrate the absorbing effect of the fine-flaked phenol resin foamed plastic at room temperature in relation to particular substances and solutions, one gram of the test material is weighed into an Erlenmeyer flask (size 250 ml).
Subsequently 10 ml of the liquid to be absorbed is added and simultaneously dispersed. After a standing period of 5 minutes, ~- the contents of the Erlenmeyer flask are poured onto a wire screen wcb. The non-absorbed portion of the liquid will drip 30 off. After a drainage period of two minutes, the non-absorbed liquid portion is measured. After dripping off of the non-absorbed portion of the liquid, the loaded chemical binder , ,, ~' .
.l . . .
J 16574~
is removed by auxiliary mecha'nical means (e.g. a blade). With higher viscosity liquids, identified ~n following Table 1 by an asterisk, a volume measurement was impractical. In these cases the addition of the liquid to be tested followed according to weight (10 9 liquid to 1 9 ch'emical binder) and only a qualitative valuation of the absorbing effect was undertaken.
With these materials it was also necessary to obtain a simultan eous mixing with the' chemical binder through mechanical dis~tri-bution with a spatula.
In each case the chemical binder, soaked with the respective test liquid, was evaluated with regard to color and quality after a storage period of 48 hours at room temperature in open vessels.
The test results are summarized in the following table.
The conversion of the tests results presented in Table I into volume and mass figures was done with the aid of literature statements concerning the packing of the absorbed liquids using as a basis a bulk density of the chemical binder of 0.15 kg per liter.
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1 ~65748 1) Evaluated 5 minutes after addition
The use of porous, hardened synthetic resin plastics obtained through the condensation of aminoplastic-or phenoplastically-formed compounds and aldehydes for the cleaning of organic solvents, which had been used as wash liquid for textile fabrics, is known from German patent DE-PS 1 132 545. For this purpose the foamed plastic acts as a filter, which absorbs the grease, odorous substances and finishing preparations washed by these solvents from the fabrics, but not the solvent cleaning agents themselves, in particular carbon tetrachloride, trichoroethylene, tetra-chloroethylene, benzol or benzene.
It has also already been suggested to use ground formalehyde resin or phenol resin foamed plastic for the absorbing and binding of oil, benzene, fat or other such chemical substances.
For purposes of catastrophe protection and other such necessary cases, to prevent acids or bases from doing harm, acids for example will be treated with sodium carbonate and thereby neutralized. This treatment with sodium carbon-ate makes it possible in many cases to add too much soda, whereby an excess of chemical caustic is then present. The neutralized product is bound by means of inorganic substances having h-igh absorption capacity. These inorganic substances with highabsorptioncapacity resulting from their containing a plurality of fine porous cells are e.g.
perlite, kieselguhr or vermiculite. The treating of a base with an acid or an acid with a base requires in addition to knowledge of chemical procedures a great deal of caution and accuracy, so that no dangerous reactions occur. Various products appear, depending on the chemicals to be neutralized, including dangerous or hazardous fumes.
~ 1 _ ~ 165748 Until now neutralization or setting of hazardous acids and bases by inorganic high porosity materials, such as the mentioned perlite, kieselguhr or vermiculite, have the further disadvantages that these materials cannot be destroyed or are destroyed only with great difficulty, since they are not combustible at customary combustion temperatures, in particular being not combustible without residue. Thus upon their subseq-uent storage or deposition the material, furthermore containing absorbed substances, as a result of the effect of water upon the substances which were initially absorbed, releases these substances whereby an additional danger is present.
The present invention is thus based upon the problem of selecting a chemical adsorbent which with an extremely high absorbing volume harmlessly takes up and unbinds acids and bases and at the same time may be destroyed through combustion practically free of residue.
SUMMARY OF THE INVENTION
In order to solve this problem, the use of phenol resin foamed plastic particles is proposed for the absorptionof bases, alcohols and radioactive liquids and acids. In addition to liquids, they can also treat such constituents which are other-wise absorbable or adherable in the foamed plastic particles.
Phenol resin foamed plastic has the capacity of absorbing and binding a large plurality of various bases and caustics to a high degree, without thereby becoming corroded to such a degree that the absorbing capacity or retaining capacity of the absorbing material suffers. The acids or bases can be of both inorganic and organic types. The phenol resin foamed plastic is also excellently suitable for the absorbing of alcohols, and even for holding radioactive liquids. A homogeneous subst-ance is accordingly capable of safely absorbing and retaining J
~ 165i48 various liquids.
In accordance with a particular embodiment of the present invention, it is suggested that a phenol resin foamed plast;c for absorbing a base be treated with an acid or be provided with accumulated acid particles, whereas a phenol resin foamed plastic destined for absorbing an acid should be treated with a base or display basic elements in its hol-low spaces, so that the neutralization of the mentioned sub-stances occurs with or within the foamed plastic. Thus a phenol resin powder or granulate for an acid neutralization in particular, is advantageously mixed with calcium carbonate.
In a a further embodiment according to the presen~
invention, it is suggested that the mentioned phenol resin foamed plastic particles be used as packing material.
According to an additional embodiment of the present invention the phenol resin foamed plastic particles in the form of powder or flakes are disposed in liquid-permeable padding, which is composed of a plastic web, in 20 particular a nylon web, or a non-woven fabric. In order to demonstrate the absorbing effect of the fine-flaked phenol resin foamed plastic at room temperature in relation to particular substances and solutions, one gram of the test material is weighed into an Erlenmeyer flask (size 250 ml).
Subsequently 10 ml of the liquid to be absorbed is added and simultaneously dispersed. After a standing period of 5 minutes, ~- the contents of the Erlenmeyer flask are poured onto a wire screen wcb. The non-absorbed portion of the liquid will drip 30 off. After a drainage period of two minutes, the non-absorbed liquid portion is measured. After dripping off of the non-absorbed portion of the liquid, the loaded chemical binder , ,, ~' .
.l . . .
J 16574~
is removed by auxiliary mecha'nical means (e.g. a blade). With higher viscosity liquids, identified ~n following Table 1 by an asterisk, a volume measurement was impractical. In these cases the addition of the liquid to be tested followed according to weight (10 9 liquid to 1 9 ch'emical binder) and only a qualitative valuation of the absorbing effect was undertaken.
With these materials it was also necessary to obtain a simultan eous mixing with the' chemical binder through mechanical dis~tri-bution with a spatula.
In each case the chemical binder, soaked with the respective test liquid, was evaluated with regard to color and quality after a storage period of 48 hours at room temperature in open vessels.
The test results are summarized in the following table.
The conversion of the tests results presented in Table I into volume and mass figures was done with the aid of literature statements concerning the packing of the absorbed liquids using as a basis a bulk density of the chemical binder of 0.15 kg per liter.
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1 ~65748 1) Evaluated 5 minutes after addition
2~ Upon addition of acetaldehyde there followed~heating ~up to about 35%C) and gas formation The test results show that the chemical binder of powdered phenol resin foamed plastic has alhigh abosrbing and binding capacity in relation to bases and caustics, alcohols and esters, as well as solvents and salt solutions.
The phenol resin foamed plastic to be powdered can be in the form of closed cells, since upon pulverization the cell borders of the pulverized portion will be opened. It is particularly advantageous for the phenol resin foam to be open-celled, since like a sponge it will have a very high absorbing capacity.
The grain size of the phenol resin foam particles is practicable within the range of about 0.25 to 70.0 mm; there-under should also be understood fragments, pieces, bars or sheets.
The phenol resin foamed plastic particles are not required to be powdered. They may be cut as sheets or bars.
Small balls may also be considered for use, in particular hollow balls of phenol resin, which are character-ized also as micro-balloons (flasks).
The novel features which are considered characteri-stic for the invention are set forth in particular in the app-ended claims. The invention itself, however, both as to its construction and its method of operation, together with addit-ional objects and advantages ~hereof, will be best understood from the following description oi` specific embodiments when read in connection with the accompanying drawing.
BRIE~ DESCRIPTION OF THE DRAWINGS
~ig. 1 is a perspective view representation of a padding;
~ r " ~ ~65748 FIG. 2 shows a packing schematically in vertical sectton, FIG. 3 shows another packing in vertical section;
FIG. 4 shows a modified padding; and FlG. 5 shows another packing.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
According to FIG. 1 the padding 10 is composed of two layers of a nylon web or a fleece, which is turned up about edge 11, and in which the borders 12. 13 and 14 are bound.
When dealing with a web of plastic, the binding of the borders follows advantageously through the use of pressure and heat.
~ When dealing with a fleece, the binding of the borders follows ; preferably through use of adhesives. Inside these two layers a powdered or flake-formed phenol-resin foamed plastic is present.
; FIG. 2 shows a container 15 with a flask 16, in which for example hydrofluoric acid is disposed. Inside the contain-er 15 the flask 16 is packed and protected by a plurality of paddings 10, lOa containing the phenol derivative.
In FIG. 3 the flask, which for example contains a plant-protecting agent, is packed and secured by particles 17 .
of the phenol resin foamed plastic.
FIG. 4 shows a padding 10 or similar casing. wall 18 of which, jn register, for example, with flask 16 in FIG. 2, is composed of.a liquid-permeable material, such as e.g. non-woven fabric or a web of cloth or plastic or a perforated plast1c foll, whereas the opposite side 19 is composed of non-liquid-per~eable material, e.g. a plastic foil. As in FIG.
.. .. .
'~ 30 3, particles 17 represent the phenol res1n foamed plastic, although ~here in powder or flake-form.
~ In FIG~ 5 the shaped bodies 17a and 17b of phenol .. ,.,~ .
~, , : I : g ., .~ , ~ .
~ 16~7~8 resin foamed plastic are adapted to the.contour of flask 16, which is to Be protected.
It will be understood that each of the elements described above, or two or more together, may also find a useful application in other types of adsorbents dif~ering from the types described above.
Whi1e the invention has been illustrated and des-cribed as embodied in a phenol resin foamed plastic adsorbent, it is not intended to be limited to the details shown, since various modifications and structural changes may be made without departing in any way from the spirit of the present invention.
~,~
:;
: ~lQ~
;
The phenol resin foamed plastic to be powdered can be in the form of closed cells, since upon pulverization the cell borders of the pulverized portion will be opened. It is particularly advantageous for the phenol resin foam to be open-celled, since like a sponge it will have a very high absorbing capacity.
The grain size of the phenol resin foam particles is practicable within the range of about 0.25 to 70.0 mm; there-under should also be understood fragments, pieces, bars or sheets.
The phenol resin foamed plastic particles are not required to be powdered. They may be cut as sheets or bars.
Small balls may also be considered for use, in particular hollow balls of phenol resin, which are character-ized also as micro-balloons (flasks).
The novel features which are considered characteri-stic for the invention are set forth in particular in the app-ended claims. The invention itself, however, both as to its construction and its method of operation, together with addit-ional objects and advantages ~hereof, will be best understood from the following description oi` specific embodiments when read in connection with the accompanying drawing.
BRIE~ DESCRIPTION OF THE DRAWINGS
~ig. 1 is a perspective view representation of a padding;
~ r " ~ ~65748 FIG. 2 shows a packing schematically in vertical sectton, FIG. 3 shows another packing in vertical section;
FIG. 4 shows a modified padding; and FlG. 5 shows another packing.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
According to FIG. 1 the padding 10 is composed of two layers of a nylon web or a fleece, which is turned up about edge 11, and in which the borders 12. 13 and 14 are bound.
When dealing with a web of plastic, the binding of the borders follows advantageously through the use of pressure and heat.
~ When dealing with a fleece, the binding of the borders follows ; preferably through use of adhesives. Inside these two layers a powdered or flake-formed phenol-resin foamed plastic is present.
; FIG. 2 shows a container 15 with a flask 16, in which for example hydrofluoric acid is disposed. Inside the contain-er 15 the flask 16 is packed and protected by a plurality of paddings 10, lOa containing the phenol derivative.
In FIG. 3 the flask, which for example contains a plant-protecting agent, is packed and secured by particles 17 .
of the phenol resin foamed plastic.
FIG. 4 shows a padding 10 or similar casing. wall 18 of which, jn register, for example, with flask 16 in FIG. 2, is composed of.a liquid-permeable material, such as e.g. non-woven fabric or a web of cloth or plastic or a perforated plast1c foll, whereas the opposite side 19 is composed of non-liquid-per~eable material, e.g. a plastic foil. As in FIG.
.. .. .
'~ 30 3, particles 17 represent the phenol res1n foamed plastic, although ~here in powder or flake-form.
~ In FIG~ 5 the shaped bodies 17a and 17b of phenol .. ,.,~ .
~, , : I : g ., .~ , ~ .
~ 16~7~8 resin foamed plastic are adapted to the.contour of flask 16, which is to Be protected.
It will be understood that each of the elements described above, or two or more together, may also find a useful application in other types of adsorbents dif~ering from the types described above.
Whi1e the invention has been illustrated and des-cribed as embodied in a phenol resin foamed plastic adsorbent, it is not intended to be limited to the details shown, since various modifications and structural changes may be made without departing in any way from the spirit of the present invention.
~,~
:;
: ~lQ~
;
Claims (23)
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. Method of absorbing bases, acids, alcohols or radioactive liquids, comprising contacting said bases, acids, alcohols or radioactive liquids with phenol resin foamed plastic particles and then destroying said particles with the absorbed bases, acids, alcohols or radio-active liquids.
2. Method of absorbing bases, acids, alcohols or radioactive liquids, comprising contacting said bases, acids, alcohols or radioactive liquids with phenol resin foamed open-celled plastic particles, said particles having a size from about 0.25 to 70 mm.
3. Method of absorbing bases, acids, alcohols or radioactive liquids, comprising contacting said bases, acids, alcohols or radioactive liquids with phenol resin foamed open-celled or closed celled plastic particles, said particles being powdered or fine flaked.
4. Method according to claim 2, wherein said phenol resin foamed open-celled plastic particles have been treated, covered or mixed with an acid for absorbing a base, or with a base for absorbing an acid.
5. Method according to claim 4, wherein said phenol resin foamed open-celled plastic particles have been mixed with calcium carbonate.
6. Method according to claim 4, wherein said phenol resin foamed, open-celled plastic particles are used in the form of packing material or as packing material.
7. Method according to claim 6, wherein said phenol resin foamed open-celled plastic particles are used disposed in liquid-permeable padding.
8. Method according to claim 7, wherein said padding is composed of a plastic web.
9. Method according to claim 8, wherein said plastic web is a nylon web.
10. Method according to claim 7, wherein said padding is composed of a non-woven fabric.
11. Method according to claim 7, wherein only the side of said padding facing material which is to be packed is liquid-permeable, the other side of said padding not being liquid-permeable.
12. Method according to claim 6, wherein said phenol resin foamed open-celled plastic particles are first pressed into shaped bodies of a chosen shape with the use of a binding agent, prior to use.
13. Method according to claim 12, wherein said binding agent is a phenol resin.
14. Method according to claim 4, wherein said phenol resin foamed open-celled plastic particles are first formed into sheets, blocks, cubes, tablets, balls or fragments for use as packing material.
15. Method according to claim 14, wherein said phenol resin foamed open-celled plastic particles are used encased in a liquid-permeable plastic web or non-woven fabric.
16. Method according to claim 4, wherein said phenol resin foamed open-celled plastic particles are used as packing material, as shaped bodies adapted in form to material which is to be packed.
17. Method according to claim 16. wherein said phenol resin foamed open-celled plastic particles are used encased in a liquid-permeable plastic web or non-woven fabric.
18. Method according to claim 4. wherein said phenol resin foamed open-celled plastic particles are used as packing material and are disposed in a partition wall of a packing.
19. Method according to claim 18, wherein the sid of said partition wall of said packing facing material which is to be packed is liquid-permeable.
20. Method of absorbing bases, acids, alcohols and radioactive liquids, comprising contacting said bases, acids, alcohols and radioactive liquids with phenol resin foamed plastic particles.
21. Method according to claim 1, for absorbing inorganic or organic bases and acids, wherein said phenol resin foamed plastic particles have a particle size from about 0.25 to 70 mm.
22. Method according to claim 1, using powdered open-celled or closed-celled phenol resin foamed plastic.
23. A method according to claim 20, using powdered or fine flaked closed celled phenol resin foamed plastic.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEP3019550.7 | 1980-05-22 | ||
| DE19803019550 DE3019550A1 (en) | 1980-05-22 | 1980-05-22 | Phenoplast foam particle use as adsorbent - for organic or inorganic bases and acids, alcohol(s) and radioactive liquid |
| DEP3115172.8 | 1981-04-15 | ||
| DE19813115172 DE3115172A1 (en) | 1981-04-15 | 1981-04-15 | Use of phenolic foam plastic particles |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1165748A true CA1165748A (en) | 1984-04-17 |
Family
ID=25785611
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000378006A Expired CA1165748A (en) | 1980-05-22 | 1981-05-21 | Synthetic chemical absorbents |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US4769084A (en) |
| EP (1) | EP0040821B1 (en) |
| CA (1) | CA1165748A (en) |
| DE (1) | DE3176900D1 (en) |
| NO (1) | NO811717L (en) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5279771A (en) * | 1990-11-05 | 1994-01-18 | Ekc Technology, Inc. | Stripping compositions comprising hydroxylamine and alkanolamine |
| US5342543A (en) * | 1991-05-28 | 1994-08-30 | Data Medical Associates, Inc. | Neutralizing absorbent for acids and bases |
| US5308497A (en) * | 1992-08-31 | 1994-05-03 | United Technologies Automotive, Inc. | Method of absorbing petroleum-based products |
| FR2699834B1 (en) * | 1992-12-29 | 1996-04-19 | Daniel Allard | AGENT ABSORBING NON-HYDRATED SUBSTANCES. |
| FR2700277A1 (en) * | 1993-01-08 | 1994-07-13 | Villoutreys De Brignac De Etie | Absorbent for non-hydrated materials e.g. fats, hydrocarbon(s) etc. |
| US7144849B2 (en) * | 1993-06-21 | 2006-12-05 | Ekc Technology, Inc. | Cleaning solutions including nucleophilic amine compound having reduction and oxidation potentials |
| US5500038A (en) * | 1994-08-30 | 1996-03-19 | W. L. Gore & Associates, Inc. | Non-particulating compact adsorbent filter |
| DE4433566B4 (en) * | 1994-09-20 | 2009-07-02 | Rench Chemie Gmbh | Use of a ground, open-cell phenolic resin foam as a spreadable chemical binder |
| US6645930B1 (en) * | 2000-07-10 | 2003-11-11 | Ekc Technology, Inc. | Clean room wipes for neutralizing caustic chemicals |
| KR100725240B1 (en) * | 2007-01-31 | 2007-06-04 | 한국스미더스 오아시스 주식회사 | Oil-absorbing foam manufacturing method, foams produced through the foam and foams using the same |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1519772A1 (en) * | 1966-10-28 | 1969-03-06 | Chem Fab Frankenthal G Schmidt | Method for absorbing oils, alcohols or the like. |
| SE322735B (en) * | 1967-05-26 | 1970-04-13 | H Fahlvik | |
| US3591422A (en) * | 1969-04-03 | 1971-07-06 | Eltra Corp | Water-activable battery utilizing absorbent open-celled material |
| US3862963A (en) * | 1972-04-26 | 1975-01-28 | Lion Fat Oil Co Ltd | Adsorbent for oils |
| FR2199776A5 (en) * | 1972-09-18 | 1974-04-12 | Inst Francais Du Petrole | |
| US4056112A (en) * | 1974-05-02 | 1977-11-01 | Calvin Calmon | Containment and removal of radioactive spills by depositing a crosslinked ion exchange composition in a dry form over region of spill |
| US4210460A (en) * | 1975-10-22 | 1980-07-01 | J. T. Baker Chemical Company | Spill control composition and use thereof |
| CA1048799A (en) * | 1976-10-05 | 1979-02-20 | Paul Preus | Barrier construction for water carried pollutants |
| FR2383224A1 (en) * | 1977-03-11 | 1978-10-06 | Inst Francais Du Petrole | PROCESS FOR ABSORBING HYDROCARBONS OR ORGANIC SOLVENTS |
| DE2721124A1 (en) * | 1977-05-11 | 1978-11-16 | Akzo Gmbh | DEVICE FOR THE SEPARATION OF MIXTURES OF INSOLUBLE LIQUIDS |
| FR2408373A1 (en) * | 1977-11-09 | 1979-06-08 | Abrahamsson Tage | FILTER INTENDED TO SEPARATE OILY PARTICLES FROM VALVE WATER |
| US4383868A (en) * | 1979-05-02 | 1983-05-17 | Braley Gordon K | Treatment of spillages of hazardous chemicals |
| US4366067A (en) * | 1980-10-20 | 1982-12-28 | Golding Gordon R | Method and apparatus for removal and recovery of oil |
-
1981
- 1981-05-20 NO NO811717A patent/NO811717L/en unknown
- 1981-05-21 EP EP81103907A patent/EP0040821B1/en not_active Expired
- 1981-05-21 DE DE8181103907T patent/DE3176900D1/en not_active Expired
- 1981-05-21 CA CA000378006A patent/CA1165748A/en not_active Expired
-
1987
- 1987-08-18 US US07/086,502 patent/US4769084A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| DE3176900D1 (en) | 1988-11-17 |
| EP0040821A1 (en) | 1981-12-02 |
| NO811717L (en) | 1981-11-23 |
| US4769084A (en) | 1988-09-06 |
| EP0040821B1 (en) | 1988-10-12 |
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